NDC Code(s) : 66915-414-01, 66915-414-04, 66915-414-03
Packager : CoValence Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

gloTriple Action SerumHydroquinone GEL
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66915-414
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYDROQUINONE(UNII: XV74C1N1AE)
(HYDROQUINONE - UNII:XV74C1N1AE) 		HYDROQUINONE20 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)1 g in 1 g
WITCH HAZEL(UNII: 101I4J0U34)1 g in 1 g
ALCOHOL(UNII: 3K9958V90M)1 g in 1 g
GLYCERIN(UNII: PDC6A3C0OX)1 g in 1 g
POLYGLYCERYL-4 ISOSTEARATE(UNII: 820DPX33S7)1 g in 1 g
GLYCOLIC ACID(UNII: 0WT12SX38S)1 g in 1 g
RETINOL(UNII: G2SH0XKK91)1 g in 1 g
POLYSORBATE 20(UNII: 7T1F30V5YH)1 g in 1 g
ASCOPHYLLUM NODOSUM(UNII: 168S4EO8YJ)1 g in 1 g
.ALPHA.-TOCOPHEROL, D-(UNII: N9PR3490H9)1 g in 1 g
TOCOTRIENOLS(UNII: KP2MW85SSQ)1 g in 1 g
ELAEIS OLEIFERA SEED OIL(UNII: 0FEX06A7KX)1 g in 1 g
GLUCONOLACTONE(UNII: WQ29KQ9POT)1 g in 1 g
XANTHAN GUM(UNII: TTV12P4NEE)1 g in 1 g
SODIUM BENZOATE(UNII: OJ245FE5EU)1 g in 1 g
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:66915-414-041 in 1 CARTON
1NDC:66915-414-0130 g in 1 BOTTLE, GLASS
2NDC:66915-414-03200000 g in 1 DRUM
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part358A 10/01/2009

PRINCIPAL DISPLAY PANEL

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PRINCIPAL DISPLAY PANEL

glōProfessional
Denver, CO 80223 Dist.
MADE IN USA
Caleel+Hayden
Naritaweg 165 1043 BW
Amsterdam Nederland

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